gudid
Primary ID: 500 AP
GRI-BAG (UDI 500 AP)
Manufactured by LABORATORIOS GRIFOLS SA
Data verified against official FDA/EUDAMED records on
Scannable UDI-DI Representation
GS1-128 UDI Barcode representation for GRI-BAG - Primary ID 500 AP
Device Regulatory Overview
The GRI-BAG (Model/Catalog Number: 500 AP) is a medical device manufactured by LABORATORIOS GRIFOLS SA. This product is indexed under FDA Product Code / Category Classification KPE within international Unique Device Identification (UDI) compliance databases.
Technical Specifications
- Model Number
- 500 AP
- Product Code / EMDN
- KPE
- Device Name
- GRI-BAG is a single-use, non-pyrogenic flexible empty container with incorporated 0.2 .m filter. It is supplied sterile in sealed peel-pack pouches and isavailable in volume capacities of 100 ml, 250 ml, 500 ml and 1000 ml. The GRI-BAG models have a twist-off valve output connector whereas the GRIBAGAP models have a conus vial output connector.
- Database Sync Date
- 2026-08-09 09:10:50
Full Regulatory Attributes
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{
"review_panel": "AN",
"gudid_di_status": "Published",
"sterilization_methods": ["EO", "Gamma"],
"rx_only": true
}
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Get API Token Access ($49/mo)Frequently Asked Questions
Who is the primary manufacturer of GRI-BAG?
The registered manufacturer of record for GRI-BAG is LABORATORIOS GRIFOLS SA.
What is the Primary UDI-DI identifier for GRI-BAG?
The Primary UDI-DI identifier registered in FDA GUDID and EUDAMED records is 500 AP.
What classification code is assigned to this device?
This device is registered under product classification code KPE.
Similar Classification Devices (KPE)
Other Devices by LABORATORIOS GRIFOLS SA
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